Manufacturing Engineer II

Mechanical aptitude.
Strong computer skills, including Microsoft Word, Microsoft Excel, Microsoft Project, Minitab, etc.
Familiarity and expertise with statistics, ability to analyze data, interpret results and write technical reports.
Knowledge of GMP and ISO regulations (Design Controls).
Comply with applicable FDA and international regulatory laws/standards and the Medtronic Code of Conduct.
Must be able to work in a dynamic environment with little supervision or daily direction.
Strong, team-oriented professional with good interpersonal skills and project management experience.
Bachelors degree required
Minimum of 2 years of relevant experience, or advanced degree with 0 years of experience.

Develops and executes validation strategy of various changes including scrap reduction, fixture improvements, supplier changes, and equipment optimization.
Develops manufacturing processes that are applicable to statistical process control and may develop those techniques.
Designs manufacturing processes, procedures and production layouts for assemblies, equipment installation, processing, machining and material handling.
Adapts machine or equipment design to factory and production conditions.
May incorporate inspection and test requirements into the production plan.
Inspects performance of machinery, equipment, and tools to verify their efficiency, and investigates and initiates corrective action of problems and deficiencies to ensure product quality.
Provides guidance regarding design concepts and specification requirements to best utilize equipment and manufacturing techniques.
Ensures processes and procedures are in compliance with regulations.
Ensures reliability, develops technical specifications for production, analyzes configuration and processing solutions, and tests product conformance to specifications.
Collaborates with research, design, development, and testing for product improvement projects.